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Publication : Altered zincergic innervation of the developing primary somatosensory cortex in monoamine oxidase-A knockout mice.

First Author  Brown CE Year  2003
Journal  Brain Res Dev Brain Res Volume  142
Issue  1 Pages  19-29
PubMed ID  12694941 Mgi Jnum  J:83142
Mgi Id  MGI:2657069 Doi  10.1016/s0165-3806(03)00008-7
Citation  Brown CE, et al. (2003) Altered zincergic innervation of the developing primary somatosensory cortex in monoamine oxidase-A knockout mice. Brain Res Dev Brain Res 142(1):19-29
abstractText  Genetic inactivation of monoamine oxidase-A (MAO-A) significantly elevates levels of serotonin (5-HT) during early development and causes a disruption in the compartmented organization of thalamocortical axon terminals in layer 4 of the somatosensory cortex. In order to determine whether corticocortical innervation of the primary somatosensory cortex is also affected by this mutation, we examined the distribution of zinc-containing axon terminals (terminals known to originate from within the cortex) in the developing somatosensory cortex of MAO-A knockout mice, at postnatal days (PD) 3, 5, 6, 8, 10, 12, 15, 28, and 60. In layer 4 of wild-type mice, histochemical staining for zinc respected barrel-specific compartments at all ages beyond PD 5. By contrast, zinc staining in MAO-A knockout mice did not exhibit signs of barrel compartmentation at any age. Across cortical layers, substantial developmental changes in the distribution of zinc-containing terminals were observed in wild-type mice up until PD 12, at which time the mature lamina-specific pattern of zinc staining was achieved. Similar changes were observed in the somatosensory cortex of MAO-A knockout mice, except that its developmental time course was significantly compressed, with zincergic innervation achieving a mature appearance by PD 8. These results provide evidence that an excess of monoamines, most likely 5-HT, dramatically perturbs the columnar organization of intracortical zincergic afferents in layer 4 and significantly accelerates the appearance of a mature laminar pattern of zinc-containing corticocortical terminals.
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